Regulation of hematopoietic stem cell differentiation by a single ubiquitin ligase-substrate complex

Nat Immunol. 2010 Mar;11(3):207-15. doi: 10.1038/ni.1839. Epub 2010 Jan 17.

Abstract

Hematopoietic stem cell (HSC) differentiation is regulated by cell-intrinsic and cell-extrinsic cues. In addition to transcriptional regulation, post-translational regulation may also control HSC differentiation. To test this hypothesis, we visualized the ubiquitin-regulated protein stability of a single transcription factor, c-Myc. The stability of c-Myc protein was indicative of HSC quiescence, and c-Myc protein abundance was controlled by the ubiquitin ligase Fbw7. Fine changes in the stability of c-Myc protein regulated the HSC gene-expression signature. Using whole-genome genomic approaches, we identified specific regulators of HSC function directly controlled by c-Myc binding; however, adult HSCs and embryonic stem cells sensed and interpreted c-Myc-regulated gene expression in distinct ways. Our studies show that a ubiquitin ligase-substrate pair can orchestrate the molecular program of HSC differentiation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Cycle / genetics
  • Cell Cycle / immunology
  • Cell Cycle Proteins / immunology
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology*
  • Chromatin Immunoprecipitation
  • Flow Cytometry
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / immunology
  • Hematopoietic Stem Cells / metabolism
  • Mice
  • Mice, Knockout
  • Proto-Oncogene Proteins c-myc / immunology
  • Ubiquitin-Protein Ligases / immunology*

Substances

  • Cell Cycle Proteins
  • Proto-Oncogene Proteins c-myc
  • Ubiquitin-Protein Ligases